UDI device identifier
Kroger Insulin Syringes 053008
UDI device identifier 00011110353238 · KROGER CO., THE
Key facts
| Primary DI | 00011110353238 |
|---|---|
| Brand name | Kroger Insulin Syringes |
| Version or model | 053008 |
| Company | KROGER CO., THE |
| DUNS number | 006999528 |
| Product code | FMF |
| GMDN term | Insulin syringe/needle, basic |
| Premarket submission | K062702 |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | Yes |
| Implantable | No |
| Publish date | Sep 24, 2016 |
| Version date | Aug 5, 2019 |
| Description | .5cc 8mm 30G Insulin Syringe, Sterile, Single-Use, 100ct |
At a glance
- None MAUDE reports citing this UDI
- Yes Linked premarket submission
- No EUDAMED counterpart found
- 1,000+ GUDID devices with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About UDI device identifiers (GUDID)
The Global Unique Device Identification Database (GUDID) holds the device identifiers (UDI-DIs) and key attributes that labelers submit to the FDA for devices that carry a unique device identifier.
Source: U.S. FDA Global Unique Device Identification Database (GUDID), via NLM AccessGUDID · Source date: